Canonical Allele Identifier: PA2826293927
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 338163
ClinVar RCV Id: RCV000371781 RCV000578148 RCV000859904 RCV001618596 RCV002265745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193984.1:p.Tyr342Cys
CA9810462
NM_001207055.1:c.1025A>G